Literature DB >> 19587959

Modern reaction-based indicator systems.

Dong-Gyu Cho1, Jonathan L Sessler.   

Abstract

Traditional analyte-specific synthetic receptors or sensors have been developed on the basis of supramolecular interactions (e.g., hydrogen bonding, electrostatics, weak coordinative bonds). Unfortunately, this approach is often subject to limitations. As a result, increasing attention within the chemical sensor community is turning to the use of analyte-specific molecular indicators, wherein substrate-triggered reactions are used to signal the presence of a given analyte. This tutorial review highlights recent reaction-based indicator systems that have been used to detect selected anions, cations, reactive oxygen species, and neutral substrates.

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Year:  2009        PMID: 19587959      PMCID: PMC2862969          DOI: 10.1039/b804436h

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  52 in total

1.  Anion Recognition and Sensing: The State of the Art and Future Perspectives.

Authors:  Paul D. Beer; Philip A. Gale
Journal:  Angew Chem Int Ed Engl       Date:  2001-02-02       Impact factor: 15.336

2.  Fluorescent probes for hydrogen peroxide based on a non-oxidative mechanism.

Authors:  Hatsuo Maeda; Yuka Fukuyasu; Shoko Yoshida; Masako Fukuda; Kanako Saeki; Hiromi Matsuno; Yuji Yamauchi; Kenji Yoshida; Kazumasa Hirata; Kazuhisa Miyamoto
Journal:  Angew Chem Int Ed Engl       Date:  2004-04-26       Impact factor: 15.336

3.  Fluorescent chemodosimeter for selective detection of cyanide in water.

Authors:  Kyung-Sik Lee; Hae-Jo Kim; Gun-Hee Kim; Injae Shin; Jong-In Hong
Journal:  Org Lett       Date:  2007-12-05       Impact factor: 6.005

4.  Oxidation state-specific fluorescent method for palladium(II) and platinum(IV) based on the catalyzed aromatic claisen rearrangement.

Authors:  Amanda L Garner; Kazunori Koide
Journal:  J Am Chem Soc       Date:  2008-12-10       Impact factor: 15.419

5.  Development of novel fluorescence probes that can reliably detect reactive oxygen species and distinguish specific species.

Authors:  Ken-ichi Setsukinai; Yasuteru Urano; Katsuko Kakinuma; Hideyuki J Majima; Tetsuo Nagano
Journal:  J Biol Chem       Date:  2002-11-04       Impact factor: 5.157

6.  A novel solid-phase synthesis of highly diverse guanidines: reactions of primary amines attached to the T2 linker.

Authors:  S Dahmen; S Bräse
Journal:  Org Lett       Date:  2000-11-16       Impact factor: 6.005

7.  Chromogenic oxazines for cyanide detection.

Authors:  Massimiliano Tomasulo; Salvatore Sortino; Andrew J P White; Françisco M Raymo
Journal:  J Org Chem       Date:  2006-01-20       Impact factor: 4.354

Review 8.  Chemical basis of inflammation-induced carcinogenesis.

Authors:  Hiroshi Ohshima; Masayuki Tatemichi; Tomohiro Sawa
Journal:  Arch Biochem Biophys       Date:  2003-09-01       Impact factor: 4.013

9.  Highly sensitive and selective chemosensor for Hg2+ based on the rhodamine fluorophore.

Authors:  Min Hee Lee; Jia-Sheng Wu; Jeong Won Lee; Jong Hwa Jung; Jong Seung Kim
Journal:  Org Lett       Date:  2007-05-26       Impact factor: 6.005

Review 10.  Neurodegenerative diseases and oxidative stress.

Authors:  Kevin J Barnham; Colin L Masters; Ashley I Bush
Journal:  Nat Rev Drug Discov       Date:  2004-03       Impact factor: 84.694

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  26 in total

1.  A rhodamine-based off-on fluorescent chemosensor for selectively sensing Cu(II) in aqueous solution.

Authors:  Ruiren Tang; Kang Lei; Ke Chen; Hua Zhao; Jingwen Chen
Journal:  J Fluoresc       Date:  2010-07-20       Impact factor: 2.217

2.  In vivo bioluminescence imaging of labile iron accumulation in a murine model of Acinetobacter baumannii infection.

Authors:  Allegra T Aron; Marie C Heffern; Zachery R Lonergan; Mark N Vander Wal; Brian R Blank; Benjamin Spangler; Yaofang Zhang; Hyo Min Park; Andreas Stahl; Adam R Renslo; Eric P Skaar; Christopher J Chang
Journal:  Proc Natl Acad Sci U S A       Date:  2017-11-14       Impact factor: 11.205

3.  A novel rhodamine-benzimidazole conjugate as a highly selective turn-on fluorescent probe for Fe(3+).

Authors:  Junbo Li; Qihui Hu; Xianglin Yu; Yang Zeng; Cancan Cao; Xiwen Liu; Jia Guo; Zhiquan Pan
Journal:  J Fluoresc       Date:  2011-05-27       Impact factor: 2.217

Review 4.  Activity-based sensing fluorescent probes for iron in biological systems.

Authors:  Allegra T Aron; Audrey G Reeves; Christopher J Chang
Journal:  Curr Opin Chem Biol       Date:  2018-01-05       Impact factor: 8.822

Review 5.  Boronate-based fluorescent probes: imaging hydrogen peroxide in living systems.

Authors:  Vivian S Lin; Bryan C Dickinson; Christopher J Chang
Journal:  Methods Enzymol       Date:  2013       Impact factor: 1.600

6.  Synthesis of 1,8-naphthyridines and their application in the development of anionic fluorogenic chemosensors.

Authors:  Celso R Nicoleti; Diogo N Garcia; Luiz E da Silva; Iêda M Begnini; Ricardo A Rebelo; Antonio C Joussef; Vanderlei G Machado
Journal:  J Fluoresc       Date:  2012-03-27       Impact factor: 2.217

7.  Design, synthesis and pH sensing properties of novel PAMAM light-harvesting dendrons based on rhodamine 6G and 1,8-naphthalimide.

Authors:  Nikolai I Georgiev; Vladimir B Bojinov; Alexandrina I Venkova
Journal:  J Fluoresc       Date:  2013-02-09       Impact factor: 2.217

8.  Quantitative Fluorescence Assays Using a Self-Powered Paper-Based Microfluidic Device and a Camera-Equipped Cellular Phone.

Authors:  Nicole K Thom; Gregory G Lewis; Kimy Yeung; Scott T Phillips
Journal:  RSC Adv       Date:  2014-01-01       Impact factor: 3.361

9.  Molecular imaging of labile iron(II) pools in living cells with a turn-on fluorescent probe.

Authors:  Ho Yu Au-Yeung; Jefferson Chan; Teera Chantarojsiri; Christopher J Chang
Journal:  J Am Chem Soc       Date:  2013-09-24       Impact factor: 15.419

Review 10.  Reaction-based small-molecule fluorescent probes for chemoselective bioimaging.

Authors:  Jefferson Chan; Sheel C Dodani; Christopher J Chang
Journal:  Nat Chem       Date:  2012-12       Impact factor: 24.427

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